Impact of release characteristics of sinomenine hydrochloride dosage forms on its pharmacokinetics in beagle dogs
AIM: To investigate the effect of release behavior of sustained-release dosage forms of sinomenine hydrochloride (SM·HCl) on its pharmacokinetics in beagle dogs. METHODS: The in vitro release behavior of two SM·HCl dosage forms, including commercial 12-h sustained-release tablets and 24-h sustained-...
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Published in | World journal of gastroenterology : WJG Vol. 11; no. 29; pp. 4547 - 4551 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Guangzhou Municipal Institute of Drug Control,Guangzhou 510160, Guangdong Province, China
07.08.2005
Department of Biopharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, Liaoning Province, China%Department of Biopharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, Liaoning Province, China Baishideng Publishing Group Inc |
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Summary: | AIM: To investigate the effect of release behavior of sustained-release dosage forms of sinomenine hydrochloride (SM·HCl) on its pharmacokinetics in beagle dogs. METHODS: The in vitro release behavior of two SM·HCl dosage forms, including commercial 12-h sustained-release tablets and 24-h sustained-release pellets prepared in our laboratory, was examined. The two dosage forms were orally administrated to beagle dogs, and then the in vivo SM.HCI pharmacokinetics was investigated and compared. RESULTS: The optimal SM·HCl sustained-release formulation was achieved by mixing slow- and rapidrelease pellets (9:1, w/w). The SM·HCl release profiles of the sustained-release pellets were scarcely influenced by the pH of the dissolution medium. Release from the 12-h sustained-release tablets was markedly quicker than that from the 24-h sustained-release pellets, the cumulative release up to 12-h was 99.9% vs68.7%. From a pharmacokinetic standpoint, the 24-h SM.HCI sustainedrelease pellets had longer tmax and lower Cmax compared to the 12-h sustained-release tablets, the tmax being 2.67±0.52 h vs 9.83±0.98 h and the Cmax being 1334.45±368.76 ng/mL vs 893.12±292.55 ng/mL, respectively. However, the AUC0-tn of two SM·HCl dosage forms was comparable and both preparations were statistically bioequivalent. Furthermore, the two preparations had good correlations between SM·HCl percentage absorption in vivoand the cumulative percentage release in vitro. CONCLUSION: The in vitro release properties of the dosage forms strongly affect their pharmacokinetic behavior in vivo. Therefore, managing the in vitro release behavior of dosage forms is a promising strategy for obtaining the optimal in vivo pharmacokinetic characteristics and safe therapeutic drug concentration-time curves. |
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Bibliography: | Sinomenine; Release behavior; Pharmacokinetics; Pellets Release behavior 14-1219/R R969.1 Sinomenine Pharmacokinetics Pellets ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Telephone: +86-24-23986321 Fax: +86-24-23986321 Correspondence to: Professor Zhong-Gui He, Mailbox 59, School of Pharmacy, Shenyang Pharmaceutical University, No. 103 Wenhua Road, Shenyang 110016, Liaoning Province, China. hezhgui@mail.sy.ln.cn Author contributions: All authors contributed equally to the work. |
ISSN: | 1007-9327 2219-2840 |
DOI: | 10.3748/wjg.v11.i29.4547 |